Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Frontiers | Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
Small supernumerary marker chromosome - Wikipedia
Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
Chromosome 15 - Wikiwand
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
Chromosome 15 - Wikipedia
Chromosome Marker - an overview | ScienceDirect Topics
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
![PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/765486dbb8123ad8cf82b66bc59c4b152d3049fe/2-Figure2-1.png "PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar")
PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar
A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
Neurodevelopmental Disorders Associated with Chromosome 15
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
IJMS | Free Full-Text | Chromosomal Microarray Study in Prader-Willi Syndrome
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review - ScienceDirect
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype | Journal of Medical Genetics
